Evidence map›Paper›PMID 39680184›Full record

ReviewPlant molecular biology2024

Evolutionary analysis of anthocyanin biosynthetic genes: insights into abiotic stress adaptation.

Sebastian Buitrago, Xinsun Yang, Lianjun Wang, Rui Pan, Wenying Zhang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Plant molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Sebastian BuitragoResearch Center of Crop Stresses Resistance Technologies/ MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River, Yangtze University, Jingzhou, 434025, China.
Xinsun YangHubei Sweet Potato Engineering and Technology Research Centre, Hubei Academy of Agricultural Sciences, Wuhan, 430064, China.
Lianjun WangHubei Sweet Potato Engineering and Technology Research Centre, Hubei Academy of Agricultural Sciences, Wuhan, 430064, China.
Rui PanResearch Center of Crop Stresses Resistance Technologies/ MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River, Yangtze University, Jingzhou, 434025, China. rui.p@yangtzeu.edu.cn.ORCID http://orcid.org/0000-0001-5807-8116
Wenying ZhangResearch Center of Crop Stresses Resistance Technologies/ MARA Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River, Yangtze University, Jingzhou, 434025, China. wyzhang@yangtzeu.edu.cn.

Funding

National Key Research and Development Program of China 2018YFD1000700,2018YFD1000705,2019YFD1001300,2019YFD1001305National Natural Science Foundation of China 32372052
6 · The paper itself

Abstract

Anthocyanin regulation can be fruitfully explored from a diverse perspective by studying distantly related model organisms. Land plants pioneers faced a huge evolutionary leap, involving substantial physiological and genetic changes. Anthocyanins have evolved alongside these changes, becoming versatile compounds capable of mitigating terrestrial challenges such as drought, salinity, extreme temperatures and high radiation. With the accessibility of whole-genome sequences from ancient plant lineages, deeper insights into the evolution of key metabolic pathways like phenylpropanoids have emerged. Despite understanding the function of anthocyanins under stress, gaps remain in uncovering the precise metabolic and regulatory mechanisms driving their overproduction under stressful conditions. For example, the regulatory effect of reactive oxygen species (ROS) on well-known transcription factors like MYBs is not fully elucidated. This manuscript presents an evolutionary analysis of the anthocyanin biosynthetic pathway to elucidate key genes. CINNAMATE 4-HYDROXYLASE (C4H) and CHALCONE ISOMERASE (CHI2) received particular attention. C4H exposes remarkable differences between aquatic and land plants, while CHI2 demonstrates substantial variation in gene copy number and sequence similarity across species. The role of transcription factors, such as MYB, and the involvement of ROS in the regulation of anthocyanin biosynthesis are discussed. Complementary gene expression analyses under abiotic stress in Arabidopsis thaliana, Selaginella moellendorffii, and Marchantia polymorpha reveal intriguing gene-stress relationships. This study highlights evolutionary trends and the regulatory complexity of anthocyanin production under abiotic stress, providing insights and opening avenues for future research.

Indexed as

AnthocyaninsEvolution, MolecularGene Expression Regulation, PlantStress, PhysiologicalAdaptation, PhysiologicalArabidopsisBiosynthetic PathwaysGenes, PlantPhylogenyPlant ProteinsReactive Oxygen SpeciesTranscription FactorsAnthocyaninsPlant ProteinsReactive Oxygen SpeciesTranscription FactorsAbiotic stressChalcone isomeraseGene family evolutionPhenylpropanoidsReactive oxygen species (ROS)

Identifiers

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.